An 8-year pragmatic observation evaluation of the benefits of allogeneic HCT in older and medically infirm patients with AML

Author:

Sorror Mohamed L.12ORCID,Gooley Ted A.34,Storer Barry E.34,Gerds Aaron T.5ORCID,Sekeres Mikkael A.6,Medeiros Bruno C.7,Wang Eunice S.8,Shami Paul J.9,Adekola Kehinde10ORCID,Luger Selina11,Baer Maria R.12,Rizzieri David A.13,Wildes Tanya M.14,Koprivnikar Jamie15,Smith Julie16,Garrison Mitchell16,Kojouri Kiarash17,Schuler Tammy A.1,Leisenring Wendy M.34ORCID,Onstad Lynn E.3,Becker Pamela S.1819ORCID,McCune Jeannine S.1819,Lee Stephanie J.12ORCID,Sandmaier Brenda M.12ORCID,Appelbaum Frederick R.12,Estey Elihu H.120

Affiliation:

1. 1Clinical Research Division, Fred Hutchinson Cancer Center, Seattle, WA

2. 2Division of Medical Oncology, Department of Medicine, University of Washington School of Medicine, Seattle, WA

3. 3Clinical Statistics Program, Clinical Research Division, Fred Hutchinson Cancer Center, Seattle, WA

4. 4Department of Biostatistics, School of Public Health, University of Washington, Seattle, WA

5. 5Leukemia & Myeloid Disorders Program, Cleveland Clinic, Cleveland, OH

6. 6Division of Hematology, Sylvester Comprehensive Cancer Center, University of Miami, Miami, FL

7. 7Division of Hematology, Department of Medicine, Stanford University, Stanford, CA

8. 8Roswell Park Comprehensive Cancer Center, Buffalo, NY

9. 9Division of Hematology and Hematologic Malignancies, Huntsman Cancer Institute, University of Utah, Salt Lake City, UT

10. 10Division of Hematology Oncology, Robert H. Lurie Comprehensive Cancer Center, Feinberg School of Medicine, Northwestern University, Chicago, IL

11. 11Abramson Cancer Center, University of Pennsylvania, Philadelphia, PA

12. 12University of Maryland Marlene and Stewart Greenebaum Comprehensive Cancer Center, Baltimore, MD

13. 13Division of Hematologic Malignancies and Cellular Therapy, Duke University Medical Center, Durham, NC

14. 14Division of Hematology & Oncology, University of Nebraska Medical Center, Omaha NE

15. 15John Theurer Cancer Center, Hackensack University Medical Center, Hackensack, NJ

16. 16Confluence Health/Wenatchee Valley Hospital and Clinic, Wenatchee, WA

17. 17Skagit Valley Hospital, Mount Vernon, WA

18. 18Division of Hematology/Oncology, University of California, Irvine, Irvine, CA

19. 19Department of Population Sciences, City of Hope, Duarte, CA

20. 20Division of Hematology, Department of Medicine, University of Washington School of Medicine, Seattle, WA

Abstract

Abstract We designed a prospective, observational study enrolling patients presenting for treatment of acute myeloid leukemia (AML) at 13 institutions to analyze associations between hematopoietic cell transplantation (HCT) and survival, quality of life (QOL), and function in: the entire cohort, those aged ≥65 years, those with high comorbidity burden, intermediate cytogenetic risk, adverse cytogenetic risk, and first complete remission with or without measurable residual disease. Patient were assessed 8 times over 2 years. Time-dependent regression models were used. Among 692 patients that were evaluable, 46% received HCT with a 2-year survival of 58%. In unadjusted models, HCT was associated with reduced risks of mortality most of the subgroups. However, after accounting for covariates associated with increased mortality (age, comorbidity burden, disease risks, frailty, impaired QOL, depression, and impaired function), the associations between HCT and longer survival disappeared in most subgroups. Although function, social life, performance status, and depressive symptoms were better for those selected for HCT, these health advantages were lost after receiving HCT. Recipients and nonrecipients of HCT similarly ranked and expected cure as main goal of therapy, whereas physicians had greater expectations for cure than the former. Accounting for health impairments negates survival benefits from HCT for AML, suggesting that the unadjusted observed benefit is mostly owing to selection of the healthier candidates. Considering patients’ overall expectations of cure but also the QOL burdens of HCT motivate the need for randomized trials to identify the best candidates for HCT. This trial was registered at www.clinicaltrials.gov as #NCT01929408.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

Reference46 articles.

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